NDC 60505-0183-01 - CARBAMAZEPINE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
60505-0183
Requested NDC
60505-0183-01
Package NDCs from labels
60505-0183-0, 60505-0183-5, 60505-0183-1, 60505-0183-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-09-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CARBAMAZEPINE - REMEDYREPACK INC.REMEDYREPACK INC.2026-09-28HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Apotex Corp.Apotex Corp.2026-08-26HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - American Health PackagingAmerican Health Packaging2026-08-26HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2026-03-25HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2026-03-20HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Golden State Medical Supply, Inc.Golden State Medical Supply, Inc.2025-11-25HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2025-07-28HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2024-04-04HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2022-06-06HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE TABLETS, USP 200 mgNuCare Pharmaceuticals,Inc.2021-02-16HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE 200mgRedPharm Drug, Inc.2021-01-13HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - A-S Medication SolutionsA-S Medication Solutions2020-01-18HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Proficient Rx LPProficient Rx LP2019-10-01HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Northwind Pharmaceuticals, LLCNorthwind Pharmaceuticals, LLC2015-03-23HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - State of Florida DOH Central PharmacyState of Florida DOH Central Pharmacy2010-05-20HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60505-0183-0CARBAMAZEPINE100 in 1 BOTTLETABLET10020
60505-0183-1CARBAMAZEPINE1000 in 1 BOTTLETABLET100020
60505-0183-5CARBAMAZEPINE500 in 1 BOTTLETABLET50020

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60505-0183CARBAMAZEPINE TABLET [APOTEX CORP.]18Current NDC, Legacy NDC, 3 package rows20240206_bf0d012f-da14-8ce3-d74f-56172cddebc5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-0183-0EA - Each60505-018322e3a572-b45e-4e44-ba52-b2b381b619ea12012-07-24
60505-0183-1EA - Each60505-018309301317-1e9a-4408-b724-90fe516c7baa12012-07-24
60505-0183-5EA - Each60505-0183bcc23229-5588-4f23-a06c-02c3a8a7231012012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [APOTEX CORP.]8
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [APOTEX CORP.]8
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [APOTEX CORP.]8
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [APOTEX CORP.]8
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [APOTEX CORP.]8
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ETHYLCELLULOSEINACTIVE INGREDIENT7Z8S9VYZ4BCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYPROMELLOSEINACTIVE INGREDIENT3NXW29V3WOCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 7 · 123 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CarbamazepineCARBAMAZEPINEApotex Corp.e91f9de3-3fdd-0a6b-71ce-53a2cc1428162026-09-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
CARBAMAZEPINECARBAMAZEPINEREMEDYREPACK INC.5f9535b1-ff6a-41b3-bbb2-efcf8fbacf4c2026-08-28Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
unii: 33CM23913M
carbamazepineCARBAMAZEPINENorthstar Rx LLCc91a5a1b-5481-445b-86e8-f10109ac39372026-08-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
CARBAMAZEPINECARBAMAZEPINEApotex Corp.bf0d012f-da14-8ce3-d74f-56172cddebc52026-08-26Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA075948
ndc (package): 60505-0183-1
ndc (package): 60505-0183-5
ndc (package): 60505-0183-0
ndc (product): 60505-0183
ndc11 (package): 60505018301
rxcui: 308979
spl id: 8a415613-aacb-217a-cf82-67ed8f5e7ceb
spl set id: bf0d012f-da14-8ce3-d74f-56172cddebc5
unii: 33CM23913M
CarbamazepineCARBAMAZEPINEAmerican Health Packaging87b87b57-021a-4cb2-9edd-6efa732c208f2026-08-25Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
Rohto All-In-OneHYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATEThe Mentholatum Company43e690e4-b381-46e3-838c-33aef5bdadde2026-08-20WarningsExact identifier
unii: 3NXW29V3WO
CarbamazepineCARBAMAZEPINEAscend Laboratories, LLCf0a254c5-bd33-4b14-b9f0-830b3438f5c62026-08-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
TegretolCARBAMAZEPINENovartis Pharmaceuticals Corporation8d409411-aa9f-4f3a-a52c-fbcb0c3ec0532026-08-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
unii: 33CM23913M
CarbatrolCARBAMAZEPINETakeda Pharmaceuticals America, Inc.bc03e499-5bac-4293-bff4-6864153a624d2026-08-17Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
Leader Dry Eye Relief Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400CARDINAL HEALTH 110, LLC. DBA LEADER2ded4bda-b3c3-4521-8701-5c8446fd148b2026-08-17WarningsExact identifier
unii: 3NXW29V3WO
CarbamazepineCARBAMAZEPINEUnichem Pharmaceuticals (USA), Inc.50ba2042-fc67-4266-a773-a30f07649a5a2026-08-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
unii: 33CM23913M
CarbamazepineCARBAMAZEPINEUmedica Laboratories USA Inc.48080efd-1781-4585-83f8-c43957ac63b32026-08-12Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
CarbamazepineCARBAMAZEPINEUmedica Laboratories USA Inc.f3465f71-8931-43b6-baea-eac7046a44002026-08-12Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
rxcui: 197441
unii: 33CM23913M
CARBAMAZEPINECARBAMAZEPINEAlembic Pharmaceuticals Inc.87d343a8-84d5-4cdd-b0a0-629311b51f112026-08-12Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
unii: 33CM23913M
Dr. Shitong Photon Energy Eye Care LiquidTETRAHYDROZOLINE HCL 0.05% HYPROMELLOSE 0.3% DR. SHITONG PHOTON ENERGY EYE CARE LIQUIDWenzhou Yuyuan Pharmaceutical Co., Ltd.58ace434-55ef-17ef-e063-6294a90aa8782026-08-10WarningsExact identifier
unii: 3NXW29V3WO
CARBAMAZEPINECARBAMAZEPINEREMEDYREPACK INC.52cf3ba9-0a7c-4809-830e-af93d15327262026-08-04Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA075948
ndc (package): 70518-3146-0
ndc (package): 70518-3146-1
ndc (package): 70518-3146-2
ndc (product): 70518-3146
rxcui: 308979
spl id: 583ae88f-f2fd-d821-e063-6294a90a7b95
spl set id: 52cf3ba9-0a7c-4809-830e-af93d1532726
unii: 33CM23913M
carbamazepineCARBAMAZEPINEZydus Lifesciences Limitedd10e5f83-56db-4bc9-8c51-150a2e3e20ea2026-08-04Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
carbamazepineCARBAMAZEPINEZydus Pharmaceuticals (USA) Inc.c5e4a25a-0137-4327-96f5-15735891ad5c2026-08-04Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
CarbamazepineCARBAMAZEPINETorrent Pharmaceuticals Limited7c4860c1-daba-4e0f-97fd-d30cbc8603a22026-08-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
CARBAMAZEPINECARBAMAZEPINETorrent Pharmaceuticals Limited97e6e175-75e8-437b-b457-ddb1ae4e857d2026-07-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 308979
unii: 33CM23913M

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.